Central Admixture Pharmacy Services recalls NORepinephrine added to 0.9% sodium chloride for potential sterility issues found during FDA inspection. Affected lots expire through July 2023.
Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Central Admixture Pharmacy Services has recalled specific lots of NORepinephrine solution due to concerns about sterility after an FDA inspection. This product is used in hospitals for intravenous administration and must be discarded if you have the affected lots.
The FDA inspection found potential sterility issues in the product, which could lead to infections if the solution is not properly sterile. This medication is intended for use in hospitals and must be handled with strict sterility protocols.
Healthcare facilities and hospitals that use this medication for intravenous administration. Patients receiving treatment with the recalled lots are at risk of infection.
Check the product label for the lot numbers listed: 37-882998 through 37-901149. The expiration dates range from April 2023 to July 2023. This product is only available by prescription for hospital use.
Look for the lot numbers listed in the recall notice: 37-882998 through 37-901149.
Immediately discard any products with the listed lot numbers if you have them.
No, the FDA found potential sterility issues in these products, so they should be discarded if you have the affected lots.
Check the product label for lot numbers between 37-882998 and 37-901149, which expire from April 2023 through July 2023.
Discard the product immediately and contact your pharmacy for further instructions.
We’ve drafted a message you can send Central Admixture Pharmacy Services to request your refund or repair — edit it as you like.
Subject: Recall D-0734-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0734-2023 from Central Admixture Pharmacy Services. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
